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发育异常性黑素细胞痣与皮肤黑色素瘤:对患者及其血亲而言,是黑色素瘤风险增加的标志。

Dysplastic melanocytic nevi and cutaneous melanoma: markers of increased melanoma risk for affected persons and blood relatives.

作者信息

Albert L S, Rhodes A R, Sober A J

机构信息

Dermatology Service, Massachusetts General Hospital, Boston.

出版信息

J Am Acad Dermatol. 1990 Jan;22(1):69-75. doi: 10.1016/0190-9622(90)70010-f.

Abstract

Dysplastic melanocytic nevi are potential precursors of cutaneous melanoma and markers of increased risk. This article presents representative case histories that illustrate the usefulness of careful follow-up of persons who have dysplastic melanocytic nevi or cutaneous melanoma, as well as examination of their blood relatives for the same lesions. Identification and periodic examination of such high-risk persons may result in the detection of melanoma in a curable phase. Our observations suggest that (1) dysplastic melanocytic nevi may aggregate in families of persons who have dysplastic melanocytic nevi or melanoma, even in the absence of a family history of dysplastic melanocytic nevi or melanoma and (2) formal genetic and natural history studies of persons who have dysplastic melanocytic nevi outside the familial melanoma setting are warranted.

摘要

发育异常性黑素细胞痣是皮肤黑素瘤的潜在前体和风险增加的标志物。本文介绍了一些具有代表性的病例史,这些病例史说明了对患有发育异常性黑素细胞痣或皮肤黑素瘤的人进行仔细随访以及检查其血亲中是否存在相同病变的有用性。识别并定期检查此类高危人群可能会在可治愈阶段发现黑素瘤。我们的观察结果表明:(1)发育异常性黑素细胞痣可能在患有发育异常性黑素细胞痣或黑素瘤的人的家族中聚集,即使没有发育异常性黑素细胞痣或黑素瘤的家族病史;(2)对家族性黑素瘤以外患有发育异常性黑素细胞痣的人进行正式的遗传学和自然史研究是必要的。

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